Clinical Research Assistant I-Minds Matter Concussion Research

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A Brief Overview

The Center for Injury Research and Prevention (CIRP) is seeking a full-time Research Assistant to support ongoing translational research in concussion care. This role requires a flexible, in-person schedule that includes both daytime and evening hours, along with the ability to travel locally to support recruitment efforts across clinical settings and community partner sites. The Research Assistant will provide essential administrative and operational support for research projects within the Minds Matter Concussion Research Program. Key responsibilities include, but are not limited to:

* Participant recruitment and study enrollment

* Data collection and entry

* Medical record abstraction

* General administrative research support

* Active participation in team meetings and collaborative activities

As a Research Assistant for the Minds Matter Concussion Program, training will be provided to support a strong aptitude for learning and future growth through professional development opportunities.

What you will do

• Provide technical and administrative support in the conduct of clinical research:
• Patient/research participant scheduling
• Patient/Research Participant screening for inclusion/exclusion criteria or case history
• Data collection
• Data entry
• Data management
• Laboratory sample processing
• Clinical research study procedures or questionnaire administration
• Organization of research records and/or other study related documentation
• Research Study Compliance
• Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials
• Comply with Institutional policies, SOPs and guidelines
• Comply with federal, state, and sponsor policies
• Additional Responsibilities may include:
• Consent subjects, with appropriate authorization and training
• Document and report adverse events
• Maintain study source documents
• Complete case report forms (paper and electronic data capture)
• Assist with IRB/regulatory submissions
• Complete case report forms or other study documentation (paper and electronic data capture)
• Follow-up care
• Order materials/supplies
• Schedule research meetings

Education Qualifications

• High School Diploma / GED Required
• Bachelor's Degree Preferred

Experience Qualifications

• Previous relevant clinical research experience Required
• At least one (1) year of relevant clinical research experience Preferred

Skills and Abilities

• Familiarity with IRB and human subject protection.

To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must receive an annual influenza vaccine. Learn more.

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SALARY RANGE:

Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.

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At CHOP, we are committed to fair and transparent pay practices. Factors such as skills and experience could result in an offer above the salary range noted in this job posting. Click here for more information regarding CHOP's Compensation and Benefits.